WO1990001033A1

WO1990001033A1 - Diorgano tin compounds and bactericides and fungicides containing them

Info

Publication number: WO1990001033A1
Application number: PCT/EP1989/000704
Authority: WO
Inventors: Horst Landsiedel; Hans Plum
Original assignee: Schering Aktiengesellschaft Berlin Und Bergkamen
Priority date: 1988-07-21
Filing date: 1989-06-22
Publication date: 1990-02-08
Also published as: DK167685B1; DK218990D0; US5149365A; FI905765A0; DE3824807A1; FI91761C; FI91761B; NZ229627A; CA1336427C; JPH04500504A; AU619872B2; AU3835589A; DK218990A; EP0428529B1; EP0428529A1; DE58902161D1

Abstract

The invention concerns new diorgano tin compounds derived from N-cyclohexyl-N'-hydroxy diazenium oxide, as well as bactericides and fungicides which are suitable as disinfectants, as preservatives for wood and other materials, for bactericidal and fungicidal finishing of textiles, plastics, building materials or as biocides for paint systems and which contain these diorgano tin compounds as active ingredients.

Description

Diorganotin compounds and these containing agents with bactericidal and fungicidal activity The invention relates to new diorganotin compounds which are derived from N-cyclohexyl-N'-hydroxy-diazenium oxide, and agents with bactericidal and fungicidal activity which act as disinfectants, wood and material preservatives, are suitable for the bactericidal and fungicidal finishing of textiles, plastics, building materials or as a biocide for painting systems and contain these diorganotin compounds as active ingredients.

The high effectiveness of triorganotin compounds against microorganisms, e.g. B. harmful fungi and bacteria is known. With trialkyltin compounds, the optimum effect is when the total C number of the alkyl groups bonded to the tin atom is 9-12. Shorter or longer alkyl groups reduce the biocidal effectiveness. Compared to the trialkyltin compounds, dialkyltin compounds have a very low biocidal activity (International Tin Research Institute, Publication No. 559, 1979; Bokranz, Plum; Progress in Chemical Research, Vol. 16, Issue 3/4, p. 377). Another group of biocides, mainly used as wood preservatives, is described in

DE-C-1 024 743. These are metal salts of

N-N'-alkyl-hydroxy-diazenium oxides or N-cyclohexyl-N'-hydroxy-diazenium oxides (abbreviated as MeHDO). A disadvantage of these compounds is that high application concentrations are required to protect the wood and the activity against wood-discoloring fungi is relatively low. For these reasons, mixtures of metal salts of N-cyclohexyl-N'-hydroxy-diazenium oxide with other biocides have been proposed to increase the effectiveness or broaden the spectrum of action (DE-A-2 336 290,

DE-A-2 341 882 and EP-B-0 072 426). It is also known that the reaction product TBT-HDO, prepared from tri-n-butyltin chloride and the potassium salt of N-cyclohexyl-N'-hydroxy-diazenium oxide (K-HDO), has a very good biocidal activity (DE- A 2 633 452).

It has now surprisingly been found that reaction products of dialkyltin compounds with N-cyclohexyl-N'-hydroxy-diazenium oxide (abbreviated as R ₂ Sn-HDO) have a very good action against bacteria and fungi, in particular also gram-negative bacteria and wood-destroying and wood-staining fungi, exhibit.

The invention relates to reaction products of dialkyltin compounds with N-cyclohexyl-N'-hydroxy-diazenium oxide (R ₂ Sn-HDO) of the general formula

in which R is an alkyl radical having 1 to 12, in particular 3-8, carbon atoms, primarily an n-alkyl radical such as n-propyl, n-butyl, n-hexyl or n-octyl, the individual radicals R being identical or can be different. The di-n-butyltin compound (R = n-butyl; DBT-HDO) is therefore particularly preferred.

The invention further relates to bactericidal and fungicidal compositions, characterized in that they contain one or more of the diorganotin compounds R ₂ Sn-HDO according to the invention, for use as wood preservatives, disinfectants, preservatives for technical products and for the biocidal finishing of textiles, plastics or building materials . The compounds R ₂ Sn-HDO are expediently used in the form of preparations such as solutions, emulsions, dispersions with and without binders or with solid carriers or diluents and, if appropriate, with the addition of wetting agents, adhesives, emulsifiers and dispersants.

Suitable solvents are e.g. B. alcohols, mineral spirits, toluene, xylene.

For the preparation of aqueous formulations, the agents according to the invention can be provided in the form of stable aqueous concentrates which contain conventional emulsifiers, preferably nonionic emulsifiers, which contain alkylaryl polyglycol ethers.

The agents according to the invention can be used excellently in the form of formulations, especially for wood protection, e.g. B. for freshly cut wood that is easily infected by bacteria and fungi such as Aspergillus and Trichoderma species; they are also suitable for the treatment of lumber, which is protected against wood-destroying fungi and also against bacterial attack by the biocidal action of the active compounds according to the invention.

Furthermore, the agents according to the invention are suitable for the biocidal finishing of aqueous coating systems, e.g. B. dispersions, with regard to in-can preservation and also to protect against attack by paint and bacteria, in particular also against the attack by aqueous wood painting systems, for. B. alkyd resin dispersions, by blue stain. Aqueous formulations for the biocidal treatment of various materials such as paper, cardboard,

Plastics, textiles, adhesives, building materials and leather are used.

Another area of application is the equipping of water fleets against unwanted microorganisms, e.g. B. for circulating cooling water, manufacturing water in paper production or drilling and cutting oils.

Depending on the area of application, the active substance concentrations are in the range of 0.1 - 5% (wood protection), 0.05 - 3% (finishing of coating systems, papers, textiles, building materials etc.) or 0.0001 - 0.2% (Cooling and make-up water, drilling and cutting oils).

The compounds according to the invention can be combined with other active compounds in order to broaden the spectrum of action, to achieve special action against special microorganisms or for insecticidal treatment. As such active ingredients are u. a .:

Copper naphthenate, copper-8-oxyquinoline, N, N'-dimethylN'-phenyl-N'-fluorodichloromethylthiosulfonyldiamide,

N-cyclohexyl-N-methoxy-2,5-dimethylfuran-3-carboxamide, 3-iodo-2-propynylbutyl-carbamate, benzimidazole-2-carbamic acid methyl ester, N-trichloromethylthiophthalimide, 1 - {[2- (2.4 -dichlorophenyl) -1,3-dioxolan-2-yl] methyl} -1H- 1,2,4-triazole, ɣ-hexachlorocyclohexane and synthetic pyrethroids such as 3- (2,2-dichlorovinyl-2,2-dimethyl) cyclopropane -1-carboxylic acid-α-cyano-3-phenoxybenzyl ester. The application or introduction of the agent can be done in any way, for. B. by brushing, spraying, dipping or by industrial methods such as pressure or vacuum impregnation.

The compounds of the invention are prepared according to the following reaction equation.

(X = halogen)

According to the invention, diorganotin halide R ₂ SnX _{2 is used} with akali salts of N-cyclohexyl-N'-hydroxy-diazenium oxide (Me-HDO) at temperatures of 50-60 ° C. in aqueous alcoholic solution or organic solvents such as. B. hexane, the product being obtained in the organic phase. The starting products can be prepared by known processes (International Tin Research Institute, Publication No. 559, 1979; Bokranz, Plum; Progress in Chemical Research, Vol. Lβ, Issue 3/4, p. 377; DE-A-26 33 452) or commercially available (SCHERING AG, BASF). The diorganotin compounds RpSn-HDO according to the invention surprisingly have a broad spectrum of action with good activity against both gram-positive and gram-negative bacteria and against wood-destroying and wood-staining fungi (Tables 1 and 2). In particular, this also applies to compounds with alkyl radicals which contain more than 4 carbon atoms, for. B. Di-n-octyltin compound. This is particularly surprising since z. B. Tri-n-octyltin compounds, in contrast to tri-n-butyltin compounds, do not show any biocidal activity. The considerably lower environmental impact of the compounds according to the invention compared to triorganotin compounds is remarkable:

As the present comparison shows, TBT-HDO, for example, releases a six-fold higher amount into the environment when stored at 65 ° C. for 6 days than with the DBT-HDO according to the invention.

As the LD ₅₀ values (po rat) show, the DBT-HDO according to the invention also shows a considerably lower toxicity to warm-blooded animals than TBT-HDO.

The toxicity to fish and daphnia in the diorganotin compounds RpDn-HDO according to the invention is orders of magnitude lower than in the triorganotin compounds R ₃ Sn-HDO.

The compounds according to the invention thus prove to be excellent active ingredients for biocidal agents with a broad spectrum of activity against harmful organisms and, at the same time, low environmental pollution. example 1

Production of bis (N-cyclohexyl-diazeniumdioxi) di-n-butyltin (DBT-HDO)

182.3 g (1 mol) of the potassium salt of N-cyclohexyl-N 'are added to a solution of 151.9 g (0.5 mol) of di-n-butyltin chloride (DBTCl) in 500 ml of methanol within about 20 minutes. -hydroxy-diazenium oxide in the form of a 30% aqueous solution. The mixture is then stirred at 50-60 ° C. for 1 h. An oily phase separates out in the lower part of the reaction vessel and is subsequently separated off and taken up in 500 ml of heptane. After drying with anhydrous sodium sulfate and filtration, the solvent is distilled off under vacuum. A solid, weakly colored, powdery product of the formula remains as a residue

Yield: 222 g (85.5% of theory) Analysis for C ₂₀ H ₄₀ N ₄ O ₄ Sn (MW: 519.26): calculated:

C: 46.26%; H: 7.77%; N: 10.79%; 0: 12.32%; Sn: 22.86% found:

C: 46.12%; H: 7.71%; N: 10.88%; 0: 12.40%; Sn: 22.90% Example 2

Production of bis (N-cyelohexyl-diazeniumdioxl) di-n-pentyltin (DPT-HDO)

The preparation was carried out analogously to Example 1 from 0.5 mol of di-n-pentyltin dichloride and 1 mol of N-cyclohexyl-N'-hydroxy-diazenium oxide.

DPT-HDO is an oily, yellow liquid.

Yield: 237 g (86.6% of theory)

Analysis for C ₂₂ H ₄₄ N ₄ O ₄ Sn (MW 547.31): calculated:

C: 48.28%; H: 8.10%; N: 10.24%; 0: 11.69%; Sn: 21.69% found:

C: 48.43%; H: 8.03%; N: 10.11%; 0: 10.60%; Sri: 21.83%

Example 3

Preparation of bis (N-cyclohexyl-diazenium dioxide) di-n-octylzlnn (DOT-HDO) The preparation was carried out analogously to Example 1 from 0.5 mol of di-n-octyltin dichloride and 1 mol of N-cyclohexyl-N'-hydroxy-diazenium oxide .

DOT-HDO is an oily, yellow liquid.

Yield: 261.7 g (82.9% of theory) Analysis for C ₂₈ H ₅₆ N ₄ O ₄ Sn (MW: 631.47): calculated:

C: 53.26%; H: 8.94%; N: 8.87%; 0: 10.13%; Sn: 18.80% found:

C: 52.35%; H: 8.82%; N: 8.96%; 0: 10.24%; Sn: 18.63%

Bactericidal effect

The bactericidal test of the compound DBT-HDO according to the invention (cf. Example 1) was carried out in the agar diffusion test (cf. Table 1). DST agar was inoculated with 1 drop of a 1:10 diluted Müller-Hinton broth of the test germs. After 2 hours of pre-diffusion at 22 ° C, the paper filters soaked in differently concentrated active ingredient solutions were put on. After 24 hours of incubation, the inhibition zones were determined (distance of the turbidity from the edge of the paper filter in mm).

Fungicidal effect

The inhibitory effect of the products according to the invention against fungi was tested in the "filter application test" (cf. Table 2). For this purpose, circular paper filters (0 5.5 cm) were soaked in ethanolic solutions with different active substance contents. After drying in a room climate, the filters were placed in Petri dishes on plate-count agar inoculated with a spore suspension. Biomalt agar 8 ° Bg was used as the nutrient medium, the incubation lasted 3 weeks at +30 ° C. The sizes of the zones of inhibition (distance of the fungal growth from the filter edge in mm) around the samples were then determined. To compare the fungicidal activity against basidiomycetes, 176 blocks of pine sapwood (5 cm × 2.5 cm × 1.5 cm, fiber direction 5 cm) with solutions of graduated concentration of the active ingredient DBT-HDO (cf. Example 1) soaked in acetone.

For comparison purposes, the starting materials di-n-butyltin dichloride and the K salt of N-cyclohexyl-N'-hydroxy-diazenium oxide were included in the investigations.

The soaked blocks were stored for 4 weeks in a climate room with an air temperature of 20 ° C and 65% relative humidity. They were then washed out in accordance with DIN EN 84. After drying, the treated blocks were installed together with an untreated reference block on a pure culture of Coniophora puteana in Kolle dishes and were thus exposed to the attack of the fungus for 16 weeks at 22 ° C. and 70% relative atmospheric humidity. The effect of the mushrooms on the individual blocks was determined by calculating the weight losses (based on the dry weights). The limit values determined in this way, which are expressed by two numbers, of which the smaller is the highest amount of protective agent (in kg / m3 wood) at which an attack has still occurred (weight loss> 3%), and the larger the lowest amount, of Table 3 shows those that have not been attacked since.

Table 3

Limits against Coniophora puteana

Leaching stress

kg of product per m ^{3 of} wood di-n-butyltin dichloride 2.8 - 4.4

K-HDO 1, 8 - 3.4

DBT-HDO 0.51-0.88

Formulation example 1

A colorless wood preservation primer containing little binder, consisting of

2.5 wt. -T1. Reaction product from Example 1,

0.2 "permethrin (ice: trans ratio 25:75),

5 "diethylene glycol monobutyl ether,

6 "long oil alkyd resin,

86.3 "white spirit, shows a good penetration ability and can be applied to the wood surface in quantities of 100 - 200 g / m ² , for example by dipping or painting.

Formulation example 2

A colored wood preservation glaze consisting of

3 parts by weight Reaction product from Example 3,

25 "long oil alkyl resin (33% phthalate resin approx.

67% triglycerides of vegetable fats), 0.5 "siccatives (Co, Mn, Pb salts),

7.8 "iron oxide red paste,

0.7 "iron oxide black paste,

5 "diethylene glycol monobutyl ether,

58 "white spirit, is suitable for painting dimensionally stable wooden components such as window frames, doors etc. Formulation example 3

An active ingredient solution for the biocidal finishing of textiles, e.g. B. cotton canvas consisting of

3.0 parts by weight. Reaction product from Example 1,

3.4 "micronized polyethylene wax,

95.6 "low-odor, synthetic isoparaffin, can be applied by spraying the solution or by dipping or soaking the materials to be treated.

Formulation example 4

A water-dilutable formulation consisting of

30 parts by weight Reaction product from Example 2,

48 "non-ionic emulsifier,

(Mixture of carboxylic acid polyglycol esters),

22 "water, mixed in the specified sequence with stirring, results in a water-dilutable preparation which can be used in concentrate ions of 1-3% by weight, for example for the fungicidal treatment of dispersions.

Claims

1. reaction products of dialkyltin compounds with

N-Cyclohexyl-N'-hydroxy-diazenium oxide of the general formula

in which R is an alkyl radical having 1 to 12 carbon atoms, where the radicals can be the same or different.

2. Dialkyltin compounds according to claim 1, characterized in that R is an n-alkyl radical having 3 to 8 carbon atoms.

3. dialkyltin compounds according to claim 1, characterized in that R is n-butyl.

4. Bactericidal and fungicidal agents, characterized in that they contain, in addition to liquid or solid carriers, one or more compounds of claims 1 to 3 as an active ingredient.

5. Wood preservative, characterized in that, in addition to liquid or solid carriers, they contain one or more compounds of claims 1 to 3 as an active ingredient.

6. Use of the agent according to claims 4 and 5 for use as wood preservative, disinfectant, preservative for technical products and for the biocidal finishing of textiles, plastics and building materials.